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  • Abstract Number: 1533 • ACR Convergence 2023

    Long-term Use of Rituximab in Systemic Sclerosis: A Real-life Italian Multicentre Study

    Giacomo De Luca1, Corrado Campochiaro2, Fabio Cacciapaglia3, Nicoletta Del Papa4, Elisabetta Zanatta5, Paolo Airò6, Maria Grazia Lazzaroni6, Dilia Giuggioli7, Maria De Santis8, Gabriella Alonzi9, Stefano Stano10, Marco Binda5, Beatrice Moccaldi5, Antonio Tonutti11, Florenzo Iannone12, Maria Antonietta D'Agostino9, Lorenzo Dagna13, marco Matucci Cerinic14 and Silvia Bosello15, 1Unit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR), IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milano, Italy, 2IRCCS San Raffaele Hospital, Unit of Immunology, Rheumatology, Allergy and Rare Disease. Vita-Salute San Raffaele University, Milan, Italy, 3Rheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari, Bari, Italy, 4Scleroderma Clinic, Dipartimento di Reumatologia, ASST Gaetano Pini CTO, Milano, Italy, 5Rheumatology Unit, Padova University Hospital, Padova, Italy, 6Rheumatology and Clinical Immunology, ASST Spedali Civili of Brescia, University of Brescia, Brescia, Italy, 7Scleroderma Unit, Rheumatology Unit, University Hospital of Modena and Reggio Emilia, Modena, Italy, 8Reumatologia e Immunologia Clinica, IRCCS Humanitas Research Hospital, Humanitas University, Rozzano, Milan, Italy, 9Scleroderma Unit, Division of Rheumatology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, 10Rheumatology Unit - DiMePRe-J University of Bari, Bari, Italy, 11Humanitas University and Humanitas Research Hospital, Rozzano, Italy, 12Rheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area, University of Bari "Aldo Moro", Bari, Italy, 13Department of Internal Medicine, IRCCS San Raffaele Hospital and Vita-Salute San Raffaele University, Milan, Italy, 14Unit of Immunology, Rheumatology, Allergy and Rare diseases, IRCCS San Raffaele Hospital, Milan, Milan, Italy, 15Division of Rheumatology - Catholic University of the Sacred Heart, Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy

    Background/Purpose: Rituximab(RTX) has been used for the management of systemic sclerosis(SSc). Its efficacy has been recently confirmed in a phase III clinical trial with extension…
  • Abstract Number: 1535 • ACR Convergence 2023

    Epidemiology and Treatment Outcome of ANCA-associated Vasculitis in South Korea: A Nationwide, Population-based Cohort Study

    Ji In Jung1, Jun Won Park2, Song Jihun3, Seulggie Choi2, Sun Jae Park3, Sang Min Park2 and Eun Young Lee4, 1Division of Rheumatology, Department of Internal Medicine, Seoul National University Hospital, Seoul, South Korea, 2Seoul National University Hospital, Seoul, South Korea, 3Seoul National University Graduate School, Seoul, South Korea, 4Seoul National University College of Medicine, Seoul, South Korea

    Background/Purpose: Previous studies on AAV have shown that the epidemiology and clinical features of GPA and MPA differ among countries. Considering their high mortality and…
  • Abstract Number: 1532 • ACR Convergence 2023

    Safety and Microvascular Effects of Long-term Treatment with Aminaphtone in Systemic Sclerosis Patients: A Retrospective Analysis

    Alberto Sulli1, Rosanna Campitiello1, Emanuele Gotelli1, Andrea Cere1, Elvis Hysa2, Tamara Vojinovic2, Carlotta Schenone1, Carmen Pizzorni1, Sabrina Paolino1, Elisa Alessandri1, Vanessa Smith3 and Maurizio Cutolo4, 1Laboratory of Experimental Rheumatology and Academic Division of Rheumatology, Department of Internal Medicine, University of Genoa, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, 2Laboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genova, Italy, 3Ghent University Hospital, Gent, Belgium, 4Laboratory of Experimental Rheumatology, Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic, Genova, Italy

    Background/Purpose: The progressive endothelial damage is one of the hallmarks of systemic sclerosis (SSc), an autoimmune connective tissue disease characterized by organ fibrotic involvement. Aminaphtone…
  • Abstract Number: 1511 • ACR Convergence 2023

    B-Cell Recovery in a Randomized Controlled Trial of B-Cell Depletion with Obinutuzumab for the Treatment of Proliferative Lupus Nephritis

    Ed Vital1, Dario Roccatello2, David Black3, Rhian Jacob-Moffatt4, Cary M. Looney5, Elsa Martins5, Huiyan (Ashley) Mao3, Thomas Schindler6, Himanshi Seghal5, Jay Garg7, Jorge Ross Terres7 and Richard Furie8, 1University of Leeds, Leeds, United Kingdom, 2University of Torino, Torino, Italy, 3Hoffmann-La Roche Ltd, Mississauga, ON, Canada, 4F. Hoffmann-La Roche Ltd, Welwyn Garden City, United Kingdom, 5F. Hoffmann-La Roche Ltd, Basel, Switzerland, 6F. Hoffmann-La Roche Ltd, Basle, Switzerland, 7Genentech, Inc., South San Francisco, CA, 8Northwell Health, Manhasset, NY

    Background/Purpose: Patients with LN who received obinutuzumab, a humanized type II anti-CD20 monoclonal antibody, with standard-of-care (MMF) immunosuppression (Phase II NOBILITY; NCT02550652; PMID 34615636) showed…
  • Abstract Number: 1543 • ACR Convergence 2023

    The Association of Frailty with Outcomes in Patients with Vasculitis

    Sebastian Sattui1, John Stadler2, Renee Borchin3, Cristina Burroughs3, Christine Yeung4, Peter Merkel4 and Robert Spiera5, 1University of Pittsburgh, Pittsburgh, PA, 2Vasculitis Foundation, Kansas City, MO, 3University of South Florida, Tampa, FL, 4University of Pennsylvania, Philadelphia, PA, 5Hosptial for Special Surgery, New York, NY

    Background/Purpose: Frailty is associated with poor health outcomes including increased risk of hospitalizations, infections, and fractures. In the baseline survey of the VascStrong study, we…
  • Abstract Number: 1544 • ACR Convergence 2023

    Increased Risk of Severe Infection in Patients with Antineutrophil Cytoplasmic Antibody-associated Vasculitides: A Population-based Trend Analysis

    Kai Zhao1, J. Antonio Avina-Zubieta2, Hui Xie3, Natasha Dehghan4 and John Esdaile2, 1Arthritis Research Canada, Coquitlam, BC, Canada, 2Arthritis Research Canada, Vancouver, BC, Canada, 3Simon Fraser University, Richmond, BC, Canada, 4University of British Columbia, Vancouver, BC, Canada

    Background/Purpose: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of multisystem inflammatory diseases. One of the most serious and common side-effects of GC and…
  • Abstract Number: 1538 • ACR Convergence 2023

    Large Vessel Involvement in Antineutrophil Cytoplasmic Antibody- Associated Vasculitis: A Single Center Experience over Two Decades

    Mahmut Kaymakci1, Mohanad Elfishawi1, Hannah Langenfeld2, Andrew Hanson2, Cynthia Crowson1, Melanie Bois1, Umar Ghaffar1, Ulrich Specks1, Matthew Koster1 and Kenneth Warrington1, 1Mayo Clinic, Rochester, MN, 2Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN

    Background/Purpose: Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) is currently categorized under the small vessel vasculitides and includes granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA),…
  • Abstract Number: 1520 • ACR Convergence 2023

    Identifying Core Domains for Clinical Trials in Systemic Sclerosis-Associated Raynaud’s Phenomenon and Digital Ulcers Using the Delphi Consensus Method

    Susanna Proudman1, Michael Hughes2, Nancy Maltez3, Edith Brown4, Virginia Hickey5, shawna grosskleg6, B Shea6, Ariane Herrick7, John Pauling8 and Peter Merkel9, 1Royal Adelaide Hospital and University of Adelaide, Adelaide, Australia, 2Northern Care Alliance NHS Foundation Trust, Salford Care Organisation, Salford, United Kingdom, 3Department of Medicine, Division of Rheumatology, The Ottawa Hospital, Ottawa, ON, Canada, 4OMERACT, Manchester, United Kingdom, 5OMERACT, Adelaide, Australia, 6OMERACT, Ottawa, ON, Canada, 7University of Manchester, Salford, United Kingdom, 8North Bristol NHS Trust, Bristol, United Kingdom, 9University of Pennsylvania, Philadelphia, PA

    Background/Purpose: The OMERACT Scleroderma Vascular Disease Working Group sought to identify essential core outcome domains for inclusion in clinical trials focusing on Raynaud's phenomenon (RP)…
  • Abstract Number: 1545 • ACR Convergence 2023

    Validation of the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria in Patients with ANCA-associated Vasculitis

    Liubov Petelytska, Vladyslav Kravchenko and Oleg Iaremenko, Bogomolets National Medical University, Kyiv, Ukraine

    Background/Purpose: The early diagnosis of ANCA-associated vasculitis (AAV) and treatment initiation may prevent progression to end organ damage, particularly renal disease. Based on the Vasculitis…
  • Abstract Number: 1518 • ACR Convergence 2023

    Efficacy and Safety of Prostaglandins Analogues in Systemic Sclerosis-associated Raynaud’s Phenomenon. a Systematic Review and Meta-Analysis

    Hana Alahmari1, Hila Jazayeri2 and Sindhu Johnson3, 1Toronto Scleroderma Program, Mount Sinai Hospital, Toronto Western Hospital, Division of Rheumatology, Department of Medicine, University of Toronto, Toronto, ON, Canada, 2University of Toronto, Toronto, ON, Canada, 3Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, ON, Canada

    Background/Purpose: Raynaud's phenomenon (RP) is a vasculopathic manifestation of Systemic Sclerosis (SSc) that can lead to digital ulceration, gangrene, autoamputation, and hand disability. Prostaglandin analogs…
  • Abstract Number: 1552 • ACR Convergence 2023

    Epidemiology and Outcome of Eosinophilic Granulomatosis with Polyangiitis in France

    Benjamin Terrier1, Camille Taillé2, Alice Brouquet3, Solenne Tauty3, Francoise Bugnard3, Loic Guillevin4, Xavier Puéchal5 and Vincent Cottin6, 1Department of Internal Medicine, Hôpital Cochin, AP-HP, Paris, France, 2AP-HP, Bichat Hospital, Reference Center for Rare Pulmonary Diseases and University of Paris Cité, Inserm 1152, Paris, France, 3Steve Consultant, Lyon, France, 4University Paris Descartes, Paris, France, 5National Referral Center for Rare Systemic Autoimmune Diseases, Paris, France, 6Coordinating Reference Center for Rare Pulmonary Diseases, Louis Pradel Hospital, University of Lyon, INRAE, Lyon, France

    Background/Purpose: Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss) belongs to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV). There are no recent data on…
  • Abstract Number: 1547 • ACR Convergence 2023

    Disease Burden of Eosinophilic Granulomatosis with Polyangiitis (EGPA): A Retrospective Analysis of US Health Insurance Claims Data

    Paul Dolin1, Danuta Kielar1, Anat Shavit1, Karina Keogh2, Jennifer Rowell1, Chris Edmonds3, Juliana Meyers4, Elizabeth Esterberg4, Tram Nham4 and Stephanie Chen5, 1AstraZeneca, Cambridge, United Kingdom, 2Mayo Clinic, Rochester, MN, 3AstraZeneca, Gaithersburg, MD, 4RTI Health Solutions, Research Triangle Park, NC, 5BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, MD

    Background/Purpose: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare necrotizing small-to-medium vessel vasculitis with a relapsing-remitting course involving prodromal (various allergic reactions), eosinophilic (infiltration into…
  • Abstract Number: 1551 • ACR Convergence 2023

    Measurement of Sinonasal Disease Activity in Granulomatosis with Polyangiitis

    Roger Yang1, Ellen Romich2, Shubhasree Banerjee3, Naomi Amudala3, Peter Merkel3, Joshua Baker3 and Rennie Rhee3, 1University of Pennsylvania, Montréal, QC, Canada, 2Hospital of the University of Pennsylvania, Media, PA, 3University of Pennsylvania, Philadelphia, PA

    Background/Purpose: In granulomatosis with polyangiitis (GPA), sinonasal inflammation can be severe and significantly impact quality of life. Little is known about the most effective local…
  • Abstract Number: 1546 • ACR Convergence 2023

    Eosinophilic Granulomatosis with Polyangiitis: Clinical Suspicion Red Flags Identification by a Systematic Literature Review and Multidisciplinary Expert Consensus

    Ricardo Blanco1, Iñigo Rúa-Figueroa2, Roser Solans3, Maria C Cid4, Marina Blanco5, Ismael Garcia Moguel6, Francisco Perez Grimaldi7, Ana Noblejas8, Moises Labrador3, Cristian Domingo9, Georgina espigol10, Fernando Sanchez Toril11, Francisco Ortiz-Sanjuán12, Ebymar Arismendi13 and Jose María Alvaro-Gracias14, 1Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain, 2Rheumatology, Hospital de Gran Canaria Doctor Negrin, Las Palmas de Gran Canaria, Spain, 3Internal Medicine Department, H. Universitari Vall d’Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain, 4Hospital Clinic Barcelona, Barcelona, Spain, 5Pneumology Department, Hospital Universitario de A Coruña, Madrid, Spain, 6Allergy Department, Hospital Universitario 12 de Octubre, Madrid, Spain; Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain, 7Pneumology Department, H. University of Jerez, Cádiz, Spain, 8Internal Medicine Department, Hospital Universitario La Paz, Madrid, Spain, 9Pneumology Department, Corporació Sanitaria Parc Taulí, Universitat Autònoma de Barcelona, Barcelona, Spain, 10Autoimmune Diseases Department, Hospital Clínic, FCRB-IDIBAPS, Universitat de Barcelona, Barcelona, Spain, 11Pneumology Department, Hospital Arnau Vilanova, Valencia, Spain;, Valencia, Spain, 12Hospital Universitario y Politécnico La Fe, Valencia, Spain, 13Pneumology Department, Hospital Clínic de Barcelona, Barcelona, Spain, Universitat de Barcelona, Spain and CIBERES, Barcelona, Spain, 14Hospital General Universitario Gregorio Marañon, Madrid, Spain

    Background/Purpose: Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare ANCA-associated vasculitis, characterized histologically by eosinophilic tissue infiltration, necrotizing vasculitis, and eosinophil-rich granulomatous inflammation. The diagnosis…
  • Abstract Number: 1472 • ACR Convergence 2023

    Prevalence of Hepatic Injury in Patients with Systemic Lupus Erythematosus: A 28-Year Single Center Experience

    Asif Hitawala1, Zerai Manna2, Yenealem Temesgen-Oyelakin3, Elaine Poncio3, Christopher Koh4, sarfaraz Hasni2 and Theo Heller4, 1NIDDK/NIH, Bethesda, MD, 2Lupus Clinical Trials Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, 3National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, 4NIDDK/Liver disease branch, Bethesda, MD

    Background/Purpose: Patients with systemic lupus erythematosus (SLE) are known to have hepatic injury (HI), however large-scale longitudinal studies are lacking.We report our experience of HI…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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